FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Precision S 4K Sinuscope

K Number: K253602 · Decision Jun 4, 2026
Classifications
1
FEI Numbers
65
Registration Numbers
65
Same Product Code
92
Applicant Total
101
Review Days
198

Basic Information

Device Name
Precision S 4K Sinuscope
K Number
K253602
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1480
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker Endoscopy
Date Received
November 18, 2025
Decision Date
June 4, 2026
Product Code
GWG
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GWG Endoscope, Neurological

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GWG), ordered by most recent decision date.

View all

Other Clearances by Stryker Endoscopy

K Number Device Name
K261037 780 nm SPY Portable Handheld Imaging (SPY-PHI) System
K260185 1688 4K Camera System with Advanced Imaging Modality; 1788 4K Camera System with Advanced Imaging Modality
K260108 L12 LED Light Source with AIM
K254014 Connected OR Hub with Device and Voice Control; SDC4K Information Management System with Device and Voice Control
K253888 MOLLI 2 System
K252010 SPY Laparoscope
K252012 SPY Cystoscope/Hysteroscope
K250544 Knotilus+ Biocomposite Knotless Anchor
K250528 Stryker AlphaVent™ Knotless SP Biocomposite Anchor
K241401 Connected OR Hub with Device and Voice Control; SDC4K Information Management System with Device and Voice Control
Search all 101 clearances from Stryker Endoscopy →